Sun Med, LLC: Medical Device Recall in 2018 - (Recall #: Z-2156-2018)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2018.

Data Source: FDA.

Product Description:

MEDLINE ADULT MANUAL RESUSCITATOR WITH MEDIUM ADULT MASK, TUBE RESERVOIR, FILTER, PEEP VALVE AND 7 FT. OXYGEN TUBING, REF CPRM1126FP

Product Classification:

Class II

Date Initiated: May 24, 2018

Date Posted: June 20, 2018

Recall Number: Z-2156-2018

Event ID: 80201

Reason for Recall:

There is a potential for the patient port retaining ring to not fully seat allowing the patient port to detach during use. This may impact air delivery to the patient.

Status: Terminated

Product Quantity: 361 cases

Code Information:

Lot Numbers: 313323, 313355, 313739, 313031, 313093, 313190 & 313272

Distribution Pattern:

IL & OH distributors

Voluntary or Mandated:

Voluntary: Firm initiated